A new method for the synthesis of some fused bicyclic B-lactams based on the completion of the molecular backbone by a free-radical C-C bond forming reaction is described. Many of the synthetic approaches to the fused bicyclic molecular backbone of B-lactam antibiotics are based on the annelation of
Synthese neuartiger β-Lactame; 8–Oxo-5–oxa-1-aza-bicyclo-[4,2,0]-octane
✍ Scribed by Lieselotte Paul; Peter Polczynski; Güunter Hilgetag
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2010
- Weight
- 140 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0044-2402
No coin nor oath required. For personal study only.
✦ Synopsis
Die als trans-Isomere anfallenden quartaren N-Acylvinyl-Loste VIII bilden farblose, wasserlosliche Verbindungen, die sich gut als schwerlosliche Pikrate charakterisieren lassen (s. Tab. 1). Nucleophile setzen aus VIII unter Aufnahme des Acylvinyl-Restes N-Methyl-Lost, I1 frei.
📜 SIMILAR VOLUMES
octane-2-osrbowllc acrds have been synthesised and shown to possess weak antibaoterial activity. We have recently desonbed2 the synthesis of the 8-oxo-l,j-drazabrcyclo [4.2.O] octane ring system. The 7-unsubstltuted free acids (l)3 were antibacterially inactrve, but it was surnusecl that a 7-aoylam